Canonical Allele Identifier: CA1321143488

Gene: TMEM237 ENO1P4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201623266T= , CM000664.2:g.201623266T=	GRCh38
NC_000002.11:g.202487989T= , CM000664.1:g.202487989T=	GRCh37
NC_000002.10:g.202196234T=	NCBI36
NG_032049.1:g.25264A=
NG_051007.1:g.917A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621467.5:c.*989A= (TMEM237)	ENSP00000480508.2:n.*989A=
ENST00000686475.1:n.2156A= (TMEM237)
ENST00000409883.7:c.*989A= (TMEM237) MANE Select	ENSP00000386264.2:n.*989A=
ENST00000409444.6:c.*989A= (TMEM237)	ENSP00000387203.2:n.*989A=
ENST00000409883.6:c.*989A= (TMEM237)	ENSP00000386264.2:n.*989A=
ENST00000416471.2:n.165A= (ENO1P4)
ENST00000495329.1:n.1355A= (TMEM237)
NM_001044385.2:c.*989A= (TMEM237)	NP_001037850.1:n.*989A=
NM_152388.3:c.*989A= (TMEM237)	NP_689601.2:n.*989A=
NM_001044385.3:c.*989A= (TMEM237) MANE Select	NP_001037850.1:n.*989A=
NM_152388.4:c.*989A= (TMEM237)	NP_689601.2:n.*989A=